# Prognostic Value of Ubiquitination-Related Genes in Ovarian Cancer and Their Correlation With Tumor Immunity

**Authors:** Shu Zhao, Xiaojing Lin, Yuying Huang, Zhongmin Kang, Huali Luo, Qizhu Zhang, Qinshan Li, Mengxing Li

PMC · DOI: 10.1155/humu/8369299 · 2025-07-15

## TL;DR

This study explores how ubiquitination-related genes affect ovarian cancer prognosis and immune response, offering new insights for precision immunotherapy.

## Contribution

A novel UbRGs-based prognostic model and insights into Ube2j1's role in ovarian cancer progression and immune modulation are presented.

## Key findings

- A UbRGs-based model effectively predicts ovarian cancer prognosis.
- UbRGs influence the tumor immune microenvironment and gene mutation patterns.
- Ube2j1 modulates ovarian cancer progression via the JAK2/STAT3/PD-L1 pathway.

## Abstract

Numerous studies have emphasized the importance of the ubiquitin–proteasome system (UPS) in the malignant progression of ovarian cancer (OC). However, whether ubiquitination-related genes (UbRGs) can be used to predict the prognosis of OC remains to be revealed. Patients with OC were divided into two clusters based on the expression of UbRGs, and prognosis was compared between the two clusters. A prognostic model was established based on UbRGs, and its predictive efficiency was validated using Kaplan–Meier (K–M) curves, receiver operating characteristic (ROC) curves, and a nomogram. Immune infiltration and gene mutation analyses were used to examine the effects of UbRGs on the prognosis of OC. The prognostic model served as a valid and independent predictor of OC prognosis. Immune infiltration revealed that the unique immune microenvironment of OC was regulated by UbRGs. Gene mutation analysis indicates that UbRGs likely influence OC malignant behavior by modulating gene mutation patterns. In addition, Ube2j1 was found to play an important role in regulating the malignant progression of OC. Furthermore, the mechanism by which Ube2j1 modulates the OC phenotype and reshapes its immune microenvironment via the JAK2/STAT3/PD-L1 pathway was elucidated, providing novel insights into the potential for ubiquitination-based immunotherapy in OC. This study provides novel insights into precision immunotherapy based on UbRGs in OC. The UbRGs-based prognostic model may help to provide novel insights for the application of ubiquitination-based immunotherapy in OC.

## Linked entities

- **Genes:** UBE2J1 (ubiquitin conjugating enzyme E2 J1) [NCBI Gene 51465], JAK2 (Janus kinase 2) [NCBI Gene 3717], STAT3 (signal transducer and activator of transcription 3) [NCBI Gene 6774], CD274 (CD274 molecule) [NCBI Gene 29126]
- **Diseases:** ovarian cancer (MONDO:0005140)

## Full-text entities

- **Genes:** UBE2J1 (ubiquitin conjugating enzyme E2 J1) [NCBI Gene 51465] {aka CGI-76, HSPC153, HSPC205, HSU93243, NCUBE-1, NCUBE1}, JAK2 (Janus kinase 2) [NCBI Gene 3717] {aka JTK10}, STAT3 (signal transducer and activator of transcription 3) [NCBI Gene 6774] {aka ADMIO, ADMIO1, APRF, HIES}, CD274 (CD274 molecule) [NCBI Gene 29126] {aka ADMIO5, B7-H, B7H1, PD-L1, PDCD1L1, PDCD1LG1}
- **Diseases:** Tumor (MESH:D009369), OC (MESH:D010051)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Figures

7 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12283211/full.md

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Source: https://tomesphere.com/paper/PMC12283211